DBCO-PEG4-VC-PAB-MMAE consists a ADC linker (DBCO-PEG4-VC-PAB) and a tubulin polymerization inhibitor MMAE (HY-15162). DBCO-PEG4-VC-PAB-MMAE can be used in the synthesis of antibody-drug conjugates (ADCs). MMAE is a synthetic derivative of dolastatin 10 and functions as a potent mitotic inhibitor by inhibiting tubulin polymerization.
性状
Solid
IC50 & Target[1][2]
Duocarmycins
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
Powder -20°C 3 years该产品在溶液状态不稳定,建议您现用现配,即刻使用。
参考文献
[1]. Okeley, et al. Intracellular Activation of SGN-35, a Potent Anti-CD30 Antibody-Drug Conjugate. Clinical Cancer Research (2010), 16(3), 888-897.
溶解度数据
In Vitro: DMSO : 150 mg/mL (90.47 mM; Need ultrasonic)配制储备液